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Gene Editing Jobs in Raleigh, NC (NOW HIRING)

Beam Therapeutics

Manufacturing Associate II

Durham, NC · On-site

$80K - $115K/yr

Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic ...

UNC-Chapel Hill

Open Rank

Chapel Hill, NC

... gene editing and data science/AI. Applicants should have a strong record of recent accomplishments as a postdoctoral fellow or sustained productivity as an established faculty member. Appointment and ...

Precision Biosciences

Manager, Accounting

Durham, NC · On-site +1

Using ARCUS, Precision is developing in vivo gene correction therapies for genetic diseases. Our team includes pioneers in genome editing, leaders in business, and a full staff of talented and ...

Precision Biosciences

Manager, Accounting

Durham, NC · On-site

Using ARCUS, Precision is developing in vivo gene correction therapies for genetic diseases. Our team includes pioneers in genome editing, leaders in business, and a full staff of talented and ...

PacBio

Senior Genomic Sales Specialist

Raleigh, NC · On-site

Become part of the new paradigm in gene sequencing and help shape the future of genomic study by ... Exceptional interpersonal, verbal communication skills, combined with excellent writing and editing ...

All JobsGene Editing JobsGene Editing Jobs in Raleigh, NC

Gene Editing information

See Raleigh, NC salary details

$34K

$69.8K

$109.8K

How much do gene editing jobs pay per year?

As of Aug 31, 2026, the average yearly pay for gene editing in Raleigh, NC is $69,785.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,000.00 and $82,600.00 per year, depending on experience, location, and employer.

What is gene editing?

A Gene Editing job involves researching, developing, and applying techniques to modify DNA in organisms to achieve desired traits or correct genetic defects. Professionals in this field work with technologies like CRISPR, TALENs, and zinc finger nucleases to edit genes for medical, agricultural, or scientific purposes. Roles may include laboratory research, therapeutic development, or regulatory compliance. Scientists in this field typically have backgrounds in genetics, molecular biology, or biotechnology.

What does gene editing do?

Professionals in Gene Editing roles often spend their days designing and executing experiments, analyzing genetic sequences, and developing new methods for modifying DNA in various organisms. You may also be responsible for maintaining detailed lab documentation, troubleshooting experimental challenges, and collaborating with interdisciplinary teams of biologists, chemists, and data analysts. Common tasks include preparing genetic constructs, operating advanced laboratory equipment, and interpreting research results to inform ongoing projects. These responsibilities are integral to driving scientific discovery and bringing new gene-editing applications to practical use.

What are the key skills and qualifications needed to thrive in gene editing?

To thrive in Gene Editing, you need a strong background in molecular biology, genetics, and biotechnology, typically supported by an advanced degree such as a PhD or MS in related fields. Familiarity with gene editing tools like CRISPR-Cas9, PCR, DNA sequencing platforms, and relevant software is essential, along with potential certifications in laboratory safety or bioinformatics. Attention to detail, strong problem-solving abilities, and collaborative communication skills are valuable for navigating complex experiments and coordinating with research teams. These competencies are vital to ensure experimental accuracy, maintain compliance with regulations, and drive innovation in this rapidly evolving scientific area.

Does gene editing have a future?

Gene editing is a rapidly advancing field with increasing applications in medicine, agriculture, and research. Professionals in gene editing roles, such as genetic engineers, are expected to see growth as new technologies like CRISPR become more widely adopted and regulations evolve. Staying current with scientific developments and acquiring relevant technical skills are important for those pursuing careers in this area.

What jobs work with gene editing?

Jobs that work with gene editing include genetic engineers, molecular biologists, biomedical researchers, and laboratory technicians. These roles involve using tools like CRISPR and other gene editing technologies in research, development, and clinical applications, often requiring a background in biology, genetics, or biotechnology. Professionals in this field typically work in research institutions, biotech companies, or healthcare settings and may need specialized training or certifications.

What are popular job titles related to Gene Editing jobs in Raleigh, NC?

For Gene Editing jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Gene Editing jobs in Raleigh, NC look for?

The top searched job categories for Gene Editing jobs in Raleigh, NC are:

Gene Editing jobs near you
Infographic showing various Gene Editing job openings in Raleigh, NC as of August 2026, with employment types broken down into 2% Internship, 77% Full Time, 17% Part Time, 1% Temporary, and 3% Contract. Highlights an 72% Physical, 5% Hybrid, and 23% Remote job distribution, with an average salary of $69,785 per year, or $33.6 per hour.

Clinical Project Management Director - Cell & Gene Therapy

Durham, NC • On-site

Jobtailor
See more jobs at Jobtailorexternal

$150 - $210/hr

Other

This job post has expired today. Applications are no longer accepted.

Job description


  • Lead the delivery of large, complex global clinical studies and multi-study programs, translating customer objectives into effective operational strategies and execution plans

  • Provide operational leadership across programs and portfolios, ensuring consistency, quality, financial performance and successful delivery of clinical milestones

  • Serve as the primary senior contact for sponsors, building trusted relationships, managing escalations and driving collaborative solutions to achieve shared goals

  • Lead and align global, matrixed teams across clinical operations, data management, safety, regulatory and other functional areas to ensure seamless execution

  • Proactively identify operational and strategic risks, implement mitigation plans and lead issue resolution efforts to maintain project momentum and performance

  • Oversee program financial performance, resource planning, forecasting, scope management and change control activities to support successful business outcomes

  • Contribute to proposal development, strategic planning and bid defense activities for large, multi-service clinical opportunities

  • Drive innovation, process optimization, and the implementation of best practices to enhance delivery efficiency, quality and customer satisfaction

  • Mentor and develop project leaders and cross-functional team members, fostering a culture of accountability, collaboration and professional growth


Requirements

  • 12-15+ years of experience in clinical research, clinical operations, and/or project leadership within the pharmaceutical, biotechnology, or CRO industry

  • Deep oncology therapeutic expertise is required, with a strong preference for experience leading Cell & Gene Therapy (CGT), CAR-T, TCR-T, gene editing or other Advanced Therapy Medicinal Product (ATMP) programs

  • Demonstrated success leading complex global oncology portfolios and building trusted relationships with executive-level stakeholders

  • Proven success leading large, global, multi-regional clinical studies, programs or portfolios with operational and financial responsibility

  • Strong understanding of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements

  • Demonstrated ability to build and maintain executive-level customer relationships and successfully manage complex stakeholder environments

  • Experience leading matrixed, cross-functional teams in a global environment

  • Strong strategic thinking, problem-solving and risk management capabilities

  • Excellent communication, presentation and influencing skills

  • Bachelor's degree in Life Sciences or a related field required; advanced degree preferred.


Core Competencies

Demonstrates extensive experience in leading complex global clinical studies and programs, with a strong focus on oncology and advanced therapy medicinal products. Proven ability to build executive-level relationships and drive operational excellence through strategic planning and risk management.


Highest-signal resume keywords

  • Clinical Research Leadership

  • Oncology Therapeutic Expertise

  • Global Clinical Operations Management

  • Stakeholder Relationship Management

  • Strategic Planning and Risk Management


ATS Optimization Keywords
Hard Skills

  • Clinical Trial Conduct

  • ICH-GCP Guidelines

  • Program Financial Performance

  • Resource Planning

  • Change Control Activities

  • Proposal Development

  • Process Optimization

  • Operational Strategy Development

  • Multi-Regional Study Management

  • Advanced Therapy Medicinal Products


Soft Skills

  • Excellent Communication

  • Presentation Skills

  • Influencing Skills

  • Problem-Solving

  • Collaboration


Industry Keywords

  • Pharmaceutical Industry

  • Biotechnology

  • CRO Industry

  • Cell & Gene Therapy

  • CAR-T

  • TCR-T

  • Gene Editing

  • Clinical Operations

  • Matrixed Teams

  • Executive-Level Stakeholders

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